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High susceptibility to experimental myopia in a mouse model with a retinal ON pathway defect
PURPOSE: Nob mice share the same mutation in the Nyx gene that is found in humans with complete congenital stationary night blindness (CSNB1). We studied nob mutant mice to determine whether this defect resulted in myopia as it does in humans. METHODS: Refractive development was measured in unmanipu...
Tallennettuna:
| Päätekijät: | , , , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2008
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2752325/ https://ncbi.nlm.nih.gov/pubmed/18235018 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1167/iovs.07-0643 |
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